| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number gain | not specified | |
| | LOC130060077, LOC130060078 +911 more | Copy number gain | Chromosome 17p13.3 duplication syndrome | |
| | | Duplication | Very long chain acyl-CoA dehydrogenase deficiency +1 more | |
| | | Deletion | Very long chain acyl-CoA dehydrogenase deficiency | |
| | | Duplication | Developmental and epileptic encephalopathy, 25 | |
| | | Copy number gain | not provided | |
| | | Duplication | Dyskeratosis congenita +1 more | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130060037, LOC130060038 +291 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
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